Page last updated: 2024-10-17

cytosine and Anhidrotic Ectodermal Dysplasia

cytosine has been researched along with Anhidrotic Ectodermal Dysplasia in 2 studies

Research Excerpts

ExcerptRelevanceReference
"Ectrodactyly-ectodermal dysplasia-clefting syndrome is an uncommon disorder that includes a clinical spectrum of limb, facial, ocular, internal ear, and urogenital malformations."1.36Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype. ( Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM, 2010)
"APECED is caused by alteration in a single gene, named the autoimmune regulator (AIRE) gene."1.32Novel compound heterozygous AIRE mutations in a Japanese patient with APECED. ( Asakura, Y; Horikawa, R; Katsumata, N; Kitanaka, S; Sato, U; Tanaka, T, 2004)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Paranaíba, LM1
Martelli-Júnior, H1
de Miranda, RT1
Bufalino, A1
Abdo Filho, RC1
Coletta, RD1
Sato, U1
Horikawa, R1
Katsumata, N1
Asakura, Y1
Kitanaka, S1
Tanaka, T1

Other Studies

2 other studies available for cytosine and Anhidrotic Ectodermal Dysplasia

ArticleYear
Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.
    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5

    Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female;

2010
Novel compound heterozygous AIRE mutations in a Japanese patient with APECED.
    Journal of pediatric endocrinology & metabolism : JPEM, 2004, Volume: 17, Issue:6

    Topics: Addison Disease; Adult; AIRE Protein; Asian People; Base Sequence; Candidiasis, Chronic Mucocutaneou

2004